The Sickle Cell Consortium is a unified platform to bring the sickle cell patient to the forefront of all matters regarding health, research, advocacy, education and awareness.
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The Sickle Cell Community Consortium is a US-based non-profit formed in 2014 to “harness and amplify the power of the patient voice”. The Consortium is comprised of sickle cell community-based organizations (CBOs), patient and caregiver advocates, community partners and medical and research advisers.